Cetirizine Hydrochloride Tablet
Product Images NDC 37835-611

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cetirizine Hydrochloride (NDC 37835-611). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bi-mar, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

14 (Label 14)

Cetirizine hydrochloride 10 mg tablets label by Bi-Mart, an OTC allergy relief medication. The label indicates 14 tablets per bottle, with the active ingredient Cetirizine HCl USP 10 mg. It highlights relief for indoor and outdoor allergy symptoms such as sneezing, runny nose, itchy or watery eyes, and itchy throat or nose. The label includes Drug Facts covering active ingredients, uses, warnings, dosage, inactive ingredients, storage, and manufacturer information.*

FDA Label Image

35 (Label 35)

Cetirizine hydrochloride 10 mg tablets by Bi-Mar, labeled as an allergy relief product. The package highlights 24-hour relief of symptoms including sneezing, runny nose, itchy/watery eyes, and itchy throat or nose. The label displays a count of 35 tablets, each 10 mg, and includes Drug Facts, directions, warnings, and inactive ingredient information.*

FDA Label Image

90 (Label 90)

Cetirizine hydrochloride 10 mg tablets by Bi-Mar, labeled as allergy relief for indoor & outdoor allergies. The package highlights 24-hour symptom relief including sneezing, runny nose, itchy watery eyes, and itchy throat or nose. The label indicates 90 tablets of 10 mg each, with instructions and warnings visible on side panels, including directions for use and inactive ingredients.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.